The role of ecological niche divergence in lineage speciation has recently stimulated the interest of evolutionary biologists and ecologists. Phylogenetic analysis has revealed that the Hyrcanian wood frog, Rana pseudodalmatina, has diverged into two western and eastern regional clades (WRC and ERC) within the Hyrcanian forest. The goal of this study was to investigate whether the ecological niches of WRC and ERC are conserved or diverged, as well as to figure out what variables promote niche conservatism or divergence. For this purpose, the maximum entropy model was employed to assess environmental niche modeling in geographical (G) space utilizing climatic and macro-environmental data. The niche overlap, equivalency, and similarity tests based on PCAenv analyses were used to assess niche divergence or conservatism in environmental (E) space. The findings strongly support the hypothesis that WRC and ERC have undergone substantial niche divergence and are constrained by a unique set of climatic and macro-environmental conditions. This study by ecological niche comparisons based on phylogenetic data provides new insights into the exploration of species diversification processes in the Hyrcanian forests.
Identifying spatial gaps in conservation networks requires information on species-environment relationships, and prioritization of habitats and corridors. We combined multi-extent niche modeling, landscape connectivity, and gap analysis to investigate scale-dependent environmental relationships, and identify core habitats and corridors for a little-known carnivore in Iran, the striped hyaena (Hyaena hyaena). This species is threatened in Iran by road vehicle collisions and direct killing. Therefore, understanding the factors that affect its habitat suitability, spatial pattern of distribution, and connectivity among them are prerequisite steps to delineate strategies aiming at human-striped hyaena co-existence. The results showed that the highest predictive power and extent of habitats was obtained at the extent sizes of 4 and 2 km, respectively. Also, connectivity analysis revealed that the extent and number of core habitats and corridors changed with increasing dispersal distance, and approximately 21% of the landscape was found to support corridors. The results of gap analysis showed that 15–17% of the core habitats overlapped with conservation areas. Given the body size of the species, its mobility, and lack of significant habitat specialization we conclude that this species would be more strongly influenced by changes in habitat amount rather than landscape configuration. Our approach showed that the scale of variables and dispersal ability must be accounted for in conservation efforts to prioritize habitats and corridors, and designing conservation areas. Our results could facilitate the conservation of striped hyaena through the identification and prioritization of habitats, establishment of conservation areas, and mitigating conflicts in corridors.
Co‐occurring carnivore species that are phylogenetically related or of similar size, morphology, and ecological needs often reduce competition by partitioning shared resources through temporal, spatial, and dietary niche segregation via behavioral adaptations. Caracals (Caracal caracal) and jungle cats (Felis chaus) co‐occur in portions of their geographical ranges and are expected to display resource segregation in these ranges. We compiled scat, stomach content, and prey remains found data from published and unpublished sources to summarize information on the diets of caracals and jungle cats across their geographical ranges during 1842–2021. We obtained 63 sources from 26 countries in Europe, Asia, and Africa, in which caracal diet included 151 species while jungle cat diet included 61 species. We found that caracals and jungle cats did not exhibit dietary niche partitioning and had greater dietary similarities in areas of range overlap. We also found that caracals consumed more diverse prey species including prey with greater average body mass compared to jungle cats. Our results suggest that greater prey diversity in areas of range overlap, caracal predation on wide range of prey, and opportunistic feeding behavior that facilitates consumption of more diverse prey species compared to jungle cats, may facilitate co‐occurrence between these two felid species.
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